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T W Prior

Showing results (31-40 of 75) with videos related to

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Human Pathology|December 9, 2000
Diffuse leiomyomatosis of the uterus: a case report with clonality analysisD Y Baschinsky, A Isa, T H Niemann, et al.
American Journal of Medical Genetics|January 30, 1995
Germline mosaicism at the fragile X locusT W Prior, A C Papp, P J Snyder, et al.
The American Journal of Pathology|August 6, 1999
Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testingR Pyatt, R B Chadwick, C K Johnson, et al.
Clinical Chemistry|January 23, 1999
Identification of MEN1 mutations in sporadic enteropancreatic neuroendocrine tumors by analysis of paraffin-embedded tissueM D Mailman, P Muscarella, W J Schirmer, et al.
African Journal of Medicine and Medical Sciences|May 31, 2001
Case report on hereditary non-polyposis colon cancer (HNPCC) in NigeriaC A Adebamowo, O Adeyi, R Pyatt, et al.
Clinical Chemistry|October 1, 1990
A model for molecular screening of newborns: simultaneous detection of Duchenne/Becker muscular dystrophies and cystic fibrosisT W Prior, W E Highsmith, K J Friedman, et al.
American Journal of Human Genetics|December 5, 1998
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy numberD W Parsons, P E McAndrew, S T Iannaccone, et al.
Human Molecular Genetics|November 1, 1996
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining geneD W Parsons, P E McAndrew, U R Monani, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 1, 1993
Evaluation of celiac disease biopsies for adenovirus 12 DNA using a multiplex polymerase chain reactionC J Vesy, J K Greenson, A C Papp, et al.
Journal of Medical Genetics|August 27, 1998
Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysisD W Parsons, P E McAndrew, P S Allinson, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Human Pathology|December 9, 2000
Diffuse leiomyomatosis of the uterus: a case report with clonality analysisD Y Baschinsky, A Isa, T H Niemann, et al.
American Journal of Medical Genetics|January 30, 1995
Germline mosaicism at the fragile X locusT W Prior, A C Papp, P J Snyder, et al.
The American Journal of Pathology|August 6, 1999
Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testingR Pyatt, R B Chadwick, C K Johnson, et al.
Clinical Chemistry|January 23, 1999
Identification of MEN1 mutations in sporadic enteropancreatic neuroendocrine tumors by analysis of paraffin-embedded tissueM D Mailman, P Muscarella, W J Schirmer, et al.
African Journal of Medicine and Medical Sciences|May 31, 2001
Case report on hereditary non-polyposis colon cancer (HNPCC) in NigeriaC A Adebamowo, O Adeyi, R Pyatt, et al.
Clinical Chemistry|October 1, 1990
A model for molecular screening of newborns: simultaneous detection of Duchenne/Becker muscular dystrophies and cystic fibrosisT W Prior, W E Highsmith, K J Friedman, et al.
American Journal of Human Genetics|December 5, 1998
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy numberD W Parsons, P E McAndrew, S T Iannaccone, et al.
Human Molecular Genetics|November 1, 1996
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining geneD W Parsons, P E McAndrew, U R Monani, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 1, 1993
Evaluation of celiac disease biopsies for adenovirus 12 DNA using a multiplex polymerase chain reactionC J Vesy, J K Greenson, A C Papp, et al.
Journal of Medical Genetics|August 27, 1998
Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysisD W Parsons, P E McAndrew, P S Allinson, et al.
Pageof 8